Medicare Program; Virtual Meeting of the Medicare Evidence Development and Coverage Advisory Committee-July 22, 2020, 35933-35935 [2020-12720]

Download as PDF Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices 35933 more tables designed to collect specific information as detailed in Table 1. TABLE 1—QUESTIONNAIRE DATA COLLECTION FORM DESIGN Tab name Description of data Introduction ............. Terms ...................... Facility Details ......... Room Area .............. EtO & EG Storage .. Sterilizer Chambers Aeration ................... APCD Summary ..... APCD Details .......... EtO Monitoring ........ Miscellaneous ......... Additional Info ......... Documents .............. Introduction and instructions for completing and submitting the questionnaire. Definitions or explanations of technical terms. Information about facility registrations, ownership, general characteristics, facility-level data. Characteristics, inventory of components, and control of individual room areas where EtO is used or emitted. Questions regarding EtO storage in drums and containers, and ethylene glycol (EG) tanks. Operation, monitoring, and control characteristics of sterilizer chambers, including chamber exhaust vents. Details of aeration equipment. Information about all air pollution control devices operated by the facility. Details regarding air pollution control devices such as scrubbers, catalytic oxidizers, thermal oxidizers, and others. Information about workspace monitoring, personal monitoring, room monitoring conducted by facility. Questions regarding facility’s wastewater treatment and other items of EtO commercial sterilization operation. Extra space to provide any additional information requested within the questionnaire. Designated fields for reporter to attach documents requested throughout the questionnaire (e.g., facility diagram; process flow diagrams; air permit; permit application documents; startup, shutdown, malfunction plan; EtO calculations and supporting information; performance tests; engineering tests; parametric monitoring; standard operating procedures; EtO monitoring results; documentation of studies done on quantifying EtO residuals in your products; and other process and instrumentation diagrams). Reporter’s information and certification for completing and submitting the questionnaire. jbell on DSKJLSW7X2PROD with NOTICES Certification ............. As described in the instructions and the questionnaire, facilities may claim certain data as CBI in their response. There is a cell in each worksheet to indicate whether the worksheet contains CBI and if so, each cell containing data being claimed as CBI should be shaded red. It should be noted that CAA section 114(c) exempts emissions data from claims of confidentiality, and emissions data provided may be made available to the public. Emissions data should not be marked confidential. A definition of what the EPA considers emissions data is provided in 40 CFR 2.301(a)(2)(i). Facilities claiming CBI must submit both a non-confidential and confidential version of their response. All nonconfidential responses to the ICR would be submitted to the EPA via email or on a thumb drive, CD–ROM, or DVD through the U.S. mail. All confidential responses to the ICR would be submitted on a thumb drive, CD–ROM, or DVD to the EPA through the U.S. mail. Non-confidential information collected from this ICR will be made available to the public. Any information designated as confidential by an ICR respondent that the EPA subsequently determines to constitute CBI or a trade secret under the EPA’s CBI regulations at 40 CFR part 2, subpart B, will be protected pursuant to those regulations and, for trade secrets, under 18 U.S.C. 1905. If no claim of confidentiality accompanies the information when it is received by the EPA, it may be made available to the public by the EPA without further notice pursuant to the EPA regulations at 40 CFR 2.203. Form numbers: None. VerDate Sep<11>2014 17:43 Jun 11, 2020 Jkt 250001 Respondents/affected entities: Facilities subject to 40 CFR part 63, subpart O. Respondent’s obligation to respond: Responses to the ICR are mandatory under the authority of section 114 of the CAA. Estimated number of respondents: 66 (total). Frequency of response: Once. Total estimated burden: The estimated cumulative respondent burden is 6,201 hours. The estimated cumulative Agency burden to administer this ICR is 1,727 hours. Burden is defined at 5 CFR 1320.03(b). Total estimated cost: The estimated cumulative costs to respondents is $569,967, including $995 operation and maintenance costs for media and postage for submitting questionnaires containing CBI. The estimated cumulative Agency costs is $100,049 including $1,440 operation and maintenance costs for data storage. Dated: June 5, 2020. Penny Lassiter, Director, Sector Policies and Programs Division. [FR Doc. 2020–12728 Filed 6–11–20; 8:45 am] BILLING CODE 6560–50–P PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [CMS–3395–N] Medicare Program; Virtual Meeting of the Medicare Evidence Development and Coverage Advisory Committee— July 22, 2020 Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Notice. AGENCY: This notice announces a virtual public meeting of the Medicare Evidence Development & Coverage Advisory Committee (MEDCAC) (‘‘Committee’’) will be held on Wednesday, July 22, 2020. This meeting will focus on the home use of noninvasive positive pressure ventilation in patients with chronic respiratory failure (CRF) consequent to chronic obstructive pulmonary disease (COPD). We are seeking the MEDCAC’s recommendations regarding the characteristics that define those patient selection and usage criteria, concomitant services, and equipment parameters necessary to best achieve positive patient health outcomes in beneficiaries with CRF consequent to COPD. This meeting is open to the public in accordance with the Federal Advisory Committee Act (5 U.S.C. App. 2, section 10(a)). DATES: Meeting Date: The virtual meeting will be held on Wednesday, July 22, 2020 from 8:00 a.m. until 4:30 p.m., Eastern Daylight Time (EDT). SUMMARY: E:\FR\FM\12JNN1.SGM 12JNN1 jbell on DSKJLSW7X2PROD with NOTICES 35934 Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices Deadline for Submission of Written Comments: Written comments must be received at the email address specified in the ADDRESSES section of this notice by 5:00 p.m., Eastern Daylight Time (EDT), on Monday, June 22, 2020. Once submitted, all comments are final. Deadlines for Speaker Registration and Presentation Materials: The deadline to register to be a speaker and to submit PowerPoint presentation materials and writings that will be used in support of an oral presentation is 5:00 p.m., EDT, on Monday, June 22, 2020. Speakers may register by phone or via email by contacting the person listed in the FOR FURTHER INFORMATION CONTACT section of this notice. Presentation materials must be received at the email address specified in the ADDRESSES section of this notice. Submission of Presentations and Comments: Presentation materials and written comments that will be presented at the meeting must be submitted via email to MedCACpresentations@ cms.hhs.gov section of this notice by Monday June 22, 2020. Deadline for All Other Attendees Registration: Individuals who want to join the meeting may register online at https://letsmeet.webex.com/letsmeet/ onstage/g.php?MTID=e6f9d4471a6f1f7 7e29f5c34c64ccdc4d by 11:59 p.m. EDT, on Sunday, July 19, 2020. Webinar and Teleconference Meeting Information: Teleconference dial-in instructions, and related webinar details will be posted on the meeting agenda, which will be available on the CMS website https://www.cms.gov/medicarecoverage-database/indexes/medcacmeetingsindex.aspx?bc=BAAAAAAAAAAA&. Participants in the MEDCAC meeting will require the following: a computer, laptop or smartphone where the WebEx application needs to be downloaded; a strong Wi-Fi or an internet connection and access to use Chrome or Firefox web browser and a webcam if the meeting participant is scheduled to speak or make a presentation during the meeting. Deadline for Submitting a Request for Special Accommodations: Individuals viewing or listening to the meeting who are hearing or visually impaired and have special requirements, or a condition that requires special assistance, should send an email to the MEDCAC Coordinator as specified in the FOR FURTHER INFORMATION CONTACT section of this notice no later than 5:00 p.m., EDT on Friday, June 26, 2020. ADDRESSES: Due to the current COVID– 19 public health emergency, the Panel meeting will be held virtually. VerDate Sep<11>2014 17:43 Jun 11, 2020 Jkt 250001 Tara Hall, MEDCAC Coordinator, via email at Tara.Hall@cms.hhs.gov or by phone 410–786–4347. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: I. Background MEDCAC, formerly known as the Medicare Coverage Advisory Committee (MCAC), is advisory in nature, with all final coverage decisions resting with CMS. MEDCAC is used to supplement CMS’ internal expertise. Accordingly, the advice rendered by the MEDCAC is most useful when it results from a process of full scientific inquiry and thoughtful discussion, in an open forum, with careful framing of recommendations and clear identification of the basis of those recommendations. MEDCAC members are valued for their background, education, and expertise in a wide variety of scientific, clinical, and other related fields. (For more information on MEDCAC, see the MEDCAC Charter (https://www.cms.gov/Regulations-andGuidance/Guidance/FACA/Downloads/ medcaccharter.pdf) and the CMS Guidance Document, Factors CMS Considers in Referring Topics to the MEDCAC (https://www.cms.gov/ medicare-coverage-database/details/ medicare-coverage-documentdetails.aspx?MCDId=10). II. Meeting Topic and Format This notice announces the Wednesday, July 22, 2020, virtual public meeting of the Committee. This meeting will focus on the home use of noninvasive positive pressure ventilation in patients with CRF consequent to COPD. Devices to be considered are home mechanical ventilators (HMVs), bi-level positive airway pressure (BPAP) devices and continuous positive airway pressure (CPAP) devices. We are seeking the MEDCAC’s recommendations regarding the characteristics that define those patient selection and usage criteria, concomitant services, and equipment parameters necessary to best achieve positive patient health outcomes in beneficiaries with CRF consequent to COPD. The MEDCAC will specifically focus on the scientific evidence associated with the outcomes most pertinent to the affected patient population. Outcomes of interest will include decreased mortality, decreased frequency of exacerbations requiring ER or hospital admission, increased time to hospital re-admission for respiratory related disease, and improved function and quality of life. Background information about this topic, including panel materials, is PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 available at https://www.cms.gov/ medicare-coverage-database/indexes/ medcac-meetingsindex.aspx?bc=BAAAAAAAAAAA&. Electronic copies of all the meeting materials will be on the CMS website no later than 2 business days before the meeting. We encourage the participation of organizations with expertise in the appraisal of the state of evidence for the use of HMV, BPAP, and CPAP equipment in the home for the affected patient population. This meeting is open to the public. The Committee will hear oral presentations from the public for approximately 60 minutes. Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than what can be reasonably accommodated during the scheduled open public hearing session, we may conduct a lottery to determine the speakers for the scheduled open public hearing session. The contact person will notify interested persons regarding their request to speak by June 29, 2020. Your comments must focus on issues specific to the list of topics that we have proposed to the Committee. The list of research topics to be discussed at the meeting will be available on the following website prior to the meeting: https://www.cms.gov/medicare-coveragedatabase/indexes/medcac-meetingsindex.aspx?bc=BAAAAAAAAAAA&. We require that you declare at the meeting whether you have any financial involvement with manufacturers (or their competitors) of any items or services being discussed. Speakers presenting at the MEDCAC meeting must include a full disclosure slide as their second slide in their presentation for financial interests (for example, type of financial association—consultant, research support, advisory board, and an indication of level, such as minor association < $10,000 or major association > $10,000) as well as intellectual conflicts of interest (for example, involvement in a federal or nonfederal advisory committee that has discussed the issue) that may pertain in any way to the subject of this meeting. If you are representing an organization, we require that you also disclose conflict of interest information for that organization. If you do not have a PowerPoint presentation, you will need to present the full disclosure information requested previously at the beginning of your statement to the Committee. The Committee will deliberate openly on the topics under consideration. Interested persons may observe the deliberations, but the Committee will E:\FR\FM\12JNN1.SGM 12JNN1 35935 Federal Register / Vol. 85, No. 114 / Friday, June 12, 2020 / Notices not hear further comments during this time except at the request of the chairperson. The Committee will also allow a 15-minute unscheduled open public session for any attendee to address issues specific to the topics under consideration. At the conclusion of the day, the members will vote and the Committee will make its recommendation(s) to CMS. III. Registration Instructions CMS’ Coverage and Analysis Group is coordinating meeting registration. While there is no registration fee, individuals must register to attend. You may register online at https://www.cms.gov/apps/ events/upcomingevents.asp?strOrder By=1&type=3 or by phone by contacting the person listed in the FOR FURTHER INFORMATION CONTACT section of this notice by the deadline listed in the DATES section of this notice. Please provide your full name (as it appears on your state-issued driver’s license), address, organization, telephone number(s), and email address. You will receive a registration confirmation with instructions for your participation at the virtual public meeting. IV. Collection of Information This document does not impose information collection requirements, that is, reporting, recordkeeping or third-party disclosure requirements. Consequently, there is no need for review by the Office of Management and Budget under the authority of the Paperwork Reduction Act of 1995 (44 U.S.C. chapter 35). The Acting Director for the Center for Clinical Standards and Quality, at the Centers for Medicare & Medicaid Services, Jean Moody-Williams, having reviewed and approved this document, authorizes Evell J. Barco Holland, who is the Federal Register Liaison, to electronically sign this document for purposes of publication in the Federal Register. Authority: 5 U.S.C. App. 2, section 10(a). Dated: June 8, 2020. Evell J. Barco Holland, Federal Register Liaison, Department of Health and Human Services. [FR Doc. 2020–12720 Filed 6–10–20; 8:45 am] BILLING CODE 4120–01–P Families, Office of Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington, DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or written, should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Administration for Native Americans (ANA) Ongoing Progress Report (OPR) and Objective Work Plan (OWP) Administration for Native Americans, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families’ (ACF) Administration for Native Americans (ANA) is requesting a revision to the information collection: Ongoing Progress Report (OPR) and the Objective Work Plan (OWP) (OMB #0970–0452). Changes are proposed to reduce the burden on the public by combining ANA’s Annual Data Report (OMB #0970–0475) with the OPR. DATES: Comments due within 60 days of publication. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, ACF is soliciting public comment on the specific aspects of the information collection described above. ADDRESSES: Copies of the proposed collection of information can be obtained and comments may be forwarded by emailing infocollection@ acf.hhs.gov. Alternatively, copies can also be obtained by writing to the Administration for Children and SUMMARY: Description: Content changes are being made to the currently approved OPR. ANA will continue to use the currently approved OPR with minimal changes to the instructions for the remainder of fiscal year (FY) 2020 and will use the modified OPR beginning FY 2021. The modified OPR combines ANA’s Annual Data Report (OMB #0970–0475) with the OPR. The information in the OPR is collected on a semi-annual basis to monitor the performance of grantees and better gauge grantee progress. The OPR information collection is conducted in accordance with Sec. 811 [42 U.S.C. 2992] of the Native American Programs Act and will allow ANA to report quantifiable results across all program areas. It also provides grantees with parameters for reporting their progress and helps ANA better monitor and determine the effectiveness of their projects. There are no changes proposed to the OWP. The OWP information collection is conducted in accordance with 42 U.S.C. of the Native American Programs Act of 1972, as amended. This collection is necessary to evaluate applications for financial assistance and determine the relative merits of the projects for which such assistance is requested, as set forth in Sec. 806 [42 U.S.C. 2991d–1](a)(1). Respondents: Federally and staterecognized tribes, Native Pacific Islanders, Tribal Colleges and Universities, native non-profits, and consortia. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Objective Work Plan ........................................................ Ongoing Progress Report FY 2020 ................................. Ongoing Progress Report FY 2021—Exp. Date ............. Total number of responses per respondent 300 200 200 Average burden hours per response 1 2 4 3 1 2 Total burden hours 900 400 1600 Annual burden hours * 300 133 533 jbell on DSKJLSW7X2PROD with NOTICES * Burden is annualized over the three year approval period. Estimated Total Annual Burden Hours: 966. Comments: The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper VerDate Sep<11>2014 17:43 Jun 11, 2020 Jkt 250001 performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information E:\FR\FM\12JNN1.SGM 12JNN1

Agencies

[Federal Register Volume 85, Number 114 (Friday, June 12, 2020)]
[Notices]
[Pages 35933-35935]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12720]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[CMS-3395-N]


Medicare Program; Virtual Meeting of the Medicare Evidence 
Development and Coverage Advisory Committee--July 22, 2020

AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: This notice announces a virtual public meeting of the Medicare 
Evidence Development & Coverage Advisory Committee (MEDCAC) 
(``Committee'') will be held on Wednesday, July 22, 2020. This meeting 
will focus on the home use of noninvasive positive pressure ventilation 
in patients with chronic respiratory failure (CRF) consequent to 
chronic obstructive pulmonary disease (COPD). We are seeking the 
MEDCAC's recommendations regarding the characteristics that define 
those patient selection and usage criteria, concomitant services, and 
equipment parameters necessary to best achieve positive patient health 
outcomes in beneficiaries with CRF consequent to COPD. This meeting is 
open to the public in accordance with the Federal Advisory Committee 
Act (5 U.S.C. App. 2, section 10(a)).

DATES: 
    Meeting Date: The virtual meeting will be held on Wednesday, July 
22, 2020 from 8:00 a.m. until 4:30 p.m., Eastern Daylight Time (EDT).

[[Page 35934]]

    Deadline for Submission of Written Comments: Written comments must 
be received at the email address specified in the ADDRESSES section of 
this notice by 5:00 p.m., Eastern Daylight Time (EDT), on Monday, June 
22, 2020. Once submitted, all comments are final.
    Deadlines for Speaker Registration and Presentation Materials: The 
deadline to register to be a speaker and to submit PowerPoint 
presentation materials and writings that will be used in support of an 
oral presentation is 5:00 p.m., EDT, on Monday, June 22, 2020. Speakers 
may register by phone or via email by contacting the person listed in 
the FOR FURTHER INFORMATION CONTACT section of this notice. 
Presentation materials must be received at the email address specified 
in the ADDRESSES section of this notice.
    Submission of Presentations and Comments: Presentation materials 
and written comments that will be presented at the meeting must be 
submitted via email to [email protected] section of this 
notice by Monday June 22, 2020.
    Deadline for All Other Attendees Registration: Individuals who want 
to join the meeting may register online at https://letsmeet.webex.com/letsmeet/onstage/g.php?MTID=e6f9d4471a6f1f77e29f5c34c64ccdc4d by 11:59 
p.m. EDT, on Sunday, July 19, 2020.
    Webinar and Teleconference Meeting Information: Teleconference 
dial-in instructions, and related webinar details will be posted on the 
meeting agenda, which will be available on the CMS website https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. Participants in the MEDCAC meeting will 
require the following: a computer, laptop or smartphone where the WebEx 
application needs to be downloaded; a strong Wi-Fi or an internet 
connection and access to use Chrome or Firefox web browser and a webcam 
if the meeting participant is scheduled to speak or make a presentation 
during the meeting.
    Deadline for Submitting a Request for Special Accommodations: 
Individuals viewing or listening to the meeting who are hearing or 
visually impaired and have special requirements, or a condition that 
requires special assistance, should send an email to the MEDCAC 
Coordinator as specified in the FOR FURTHER INFORMATION CONTACT section 
of this notice no later than 5:00 p.m., EDT on Friday, June 26, 2020.

ADDRESSES: Due to the current COVID-19 public health emergency, the 
Panel meeting will be held virtually.

FOR FURTHER INFORMATION CONTACT: Tara Hall, MEDCAC Coordinator, via 
email at [email protected] or by phone 410-786-4347.

SUPPLEMENTARY INFORMATION: 

I. Background

    MEDCAC, formerly known as the Medicare Coverage Advisory Committee 
(MCAC), is advisory in nature, with all final coverage decisions 
resting with CMS. MEDCAC is used to supplement CMS' internal expertise. 
Accordingly, the advice rendered by the MEDCAC is most useful when it 
results from a process of full scientific inquiry and thoughtful 
discussion, in an open forum, with careful framing of recommendations 
and clear identification of the basis of those recommendations. MEDCAC 
members are valued for their background, education, and expertise in a 
wide variety of scientific, clinical, and other related fields. (For 
more information on MEDCAC, see the MEDCAC Charter (https://www.cms.gov/Regulations-and-Guidance/Guidance/FACA/Downloads/medcaccharter.pdf) and 
the CMS Guidance Document, Factors CMS Considers in Referring Topics to 
the MEDCAC (https://www.cms.gov/medicare-coverage-database/details/medicare-coverage-document-details.aspx?MCDId=10).

II. Meeting Topic and Format

    This notice announces the Wednesday, July 22, 2020, virtual public 
meeting of the Committee. This meeting will focus on the home use of 
noninvasive positive pressure ventilation in patients with CRF 
consequent to COPD. Devices to be considered are home mechanical 
ventilators (HMVs), bi-level positive airway pressure (BPAP) devices 
and continuous positive airway pressure (CPAP) devices. We are seeking 
the MEDCAC's recommendations regarding the characteristics that define 
those patient selection and usage criteria, concomitant services, and 
equipment parameters necessary to best achieve positive patient health 
outcomes in beneficiaries with CRF consequent to COPD. The MEDCAC will 
specifically focus on the scientific evidence associated with the 
outcomes most pertinent to the affected patient population. Outcomes of 
interest will include decreased mortality, decreased frequency of 
exacerbations requiring ER or hospital admission, increased time to 
hospital re-admission for respiratory related disease, and improved 
function and quality of life.
    Background information about this topic, including panel materials, 
is available at https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. Electronic copies of all 
the meeting materials will be on the CMS website no later than 2 
business days before the meeting. We encourage the participation of 
organizations with expertise in the appraisal of the state of evidence 
for the use of HMV, BPAP, and CPAP equipment in the home for the 
affected patient population. This meeting is open to the public. The 
Committee will hear oral presentations from the public for 
approximately 60 minutes. Time allotted for each presentation may be 
limited. If the number of registrants requesting to speak is greater 
than what can be reasonably accommodated during the scheduled open 
public hearing session, we may conduct a lottery to determine the 
speakers for the scheduled open public hearing session. The contact 
person will notify interested persons regarding their request to speak 
by June 29, 2020. Your comments must focus on issues specific to the 
list of topics that we have proposed to the Committee. The list of 
research topics to be discussed at the meeting will be available on the 
following website prior to the meeting: https://www.cms.gov/medicare-coverage-database/indexes/medcac-meetings-index.aspx?bc=BAAAAAAAAAAA&. 
We require that you declare at the meeting whether you have any 
financial involvement with manufacturers (or their competitors) of any 
items or services being discussed. Speakers presenting at the MEDCAC 
meeting must include a full disclosure slide as their second slide in 
their presentation for financial interests (for example, type of 
financial association--consultant, research support, advisory board, 
and an indication of level, such as minor association < $10,000 or 
major association > $10,000) as well as intellectual conflicts of 
interest (for example, involvement in a federal or nonfederal advisory 
committee that has discussed the issue) that may pertain in any way to 
the subject of this meeting. If you are representing an organization, 
we require that you also disclose conflict of interest information for 
that organization. If you do not have a PowerPoint presentation, you 
will need to present the full disclosure information requested 
previously at the beginning of your statement to the Committee.
    The Committee will deliberate openly on the topics under 
consideration. Interested persons may observe the deliberations, but 
the Committee will

[[Page 35935]]

not hear further comments during this time except at the request of the 
chairperson. The Committee will also allow a 15-minute unscheduled open 
public session for any attendee to address issues specific to the 
topics under consideration. At the conclusion of the day, the members 
will vote and the Committee will make its recommendation(s) to CMS.

III. Registration Instructions

    CMS' Coverage and Analysis Group is coordinating meeting 
registration. While there is no registration fee, individuals must 
register to attend. You may register online at https://www.cms.gov/apps/events/upcomingevents.asp?strOrderBy=1&type=3 or by phone by contacting 
the person listed in the FOR FURTHER INFORMATION CONTACT section of 
this notice by the deadline listed in the DATES section of this notice. 
Please provide your full name (as it appears on your state-issued 
driver's license), address, organization, telephone number(s), and 
email address. You will receive a registration confirmation with 
instructions for your participation at the virtual public meeting.

IV. Collection of Information

    This document does not impose information collection requirements, 
that is, reporting, recordkeeping or third-party disclosure 
requirements. Consequently, there is no need for review by the Office 
of Management and Budget under the authority of the Paperwork Reduction 
Act of 1995 (44 U.S.C. chapter 35).
    The Acting Director for the Center for Clinical Standards and 
Quality, at the Centers for Medicare & Medicaid Services, Jean Moody-
Williams, having reviewed and approved this document, authorizes Evell 
J. Barco Holland, who is the Federal Register Liaison, to 
electronically sign this document for purposes of publication in the 
Federal Register.

    Authority: 5 U.S.C. App. 2, section 10(a).

    Dated: June 8, 2020.
Evell J. Barco Holland,
Federal Register Liaison, Department of Health and Human Services.
[FR Doc. 2020-12720 Filed 6-10-20; 8:45 am]
BILLING CODE 4120-01-P


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